Lupus Foundation of Jamaica

Lupus Foundation of Jamaica Using knowledge & support to combat this disease...Spreading Lupus awareness in Jamaica Lupus butterflies are different from all other butterflies.

We have the ability to flap our wings against the wind and ascend to great heights even though our wings are often achy... or sometimes broken. Ƹ̵̡Ӝ̵̨̄Ʒ...♪♫.¸¸♥Butterfly fly away♥¸¸.♫♪...Ƹ̵Ӝ̵̨̄Ʒ

27/06/2025
Happy birthday to our talented and amazing ED! 💜You have done this job with passion, conviction, and the enthusiasm that...
05/06/2025

Happy birthday to our talented and amazing ED! 💜
You have done this job with passion, conviction, and the enthusiasm that can only come when one is truly passionate about their endeavour. You have given us your all. we see the work and the late nights, and we are eternally grateful at the love displayed through your actions.
We love you! And we are ready for an even more prosperous and exciting next chapter, not just as Executive Director of the Lupus Foubdation but as Tishuna Mullings and all the great things you are called to do.

  | Celebrating Kimley ForbesAs May draws to a close and we reflect on the heart and hustle behind our World Lupus Day a...
30/05/2025

| Celebrating Kimley Forbes

As May draws to a close and we reflect on the heart and hustle behind our World Lupus Day activities, we are pausing to celebrate someone special on the team.

Happy belated birthday to our Office Administrator, Kimley Forbes. She is often the quiet force in the background, keeping our documents in order, pulling information together, answering the helpline, and supporting our events with a willing heart.

She is dependable, steady, and brings a spirit of care to her work that keeps our operations moving. She holds a space that often goes unseen but is always deeply felt.

We are grateful for you, Kimley. Thank you for the way you show up and serve.

This moment captured in a hug is just a glimpse of the appreciation we have. Wishing you continued joy, strength and favour in the year ahead.

💜

On behalf of the Lupus Foundation of Jamaica, we extend our heartfelt thanks for your powerful support and participation...
12/05/2025

On behalf of the Lupus Foundation of Jamaica, we extend our heartfelt thanks for your powerful support and participation in World Lupus Day 2025. Your commitment helped us shine a light on the realities of lupus and brought hope and visibility to the warriors who live with this condition every day.

As we continue the journey toward better care, deeper understanding, and stronger advocacy, we invite you to remain a part of our movement. Let us continue to work together to transform lives, one step at a time so we can "MAKE LUPUS VISIBLE"💜

To stay connected or learn more about how you can support please visit our website: www.lupusfoundationjamaica.org

The Lupus Foundation of Jamaica proudly and passionately extends our warmest congratulations to the Jamaica Civil Servic...
07/05/2025

The Lupus Foundation of Jamaica proudly and passionately extends our warmest congratulations to the Jamaica Civil Service Association (JCSA) on the occasion of your 106th Anniversary.

For over a century, you have been the unwavering voice and backbone of Jamaica’s public service — protecting, empowering, and advancing the lives of thousands who serve our nation with dedication and heart. Today, we celebrate not just your longevity, but your legacy of leadership, advocacy, and people-centred service.

We are especially moved and grateful that, in marking this milestone, you chose to extend your care to us with a Corporate Social Responsibility giveback of $50,000 to the Lupus Foundation of Jamaica. This act is not just generous — it is deeply meaningful.

More than 6,000 Jamaicans are currently living with lupus — an often invisible and misunderstood illness. The majority are women between the ages of 15 and 44, in the prime of their productive years, often juggling work, family, and the physical and emotional toll of a chronic illness. But we must also shine a light on the men and boys living with lupus — often overlooked, yet equally affected — who face unique challenges in receiving support and being heard.

Your support signals that no one is forgotten. It tells Lupus Warriors in the public sector and beyond that they are seen, valued, and worthy of care.

A special salute to Yannick Sanco-Valentine, a Lupus Warrior, chapter leader, and proud JCSA member, whose courage and commitment helped inspire this generous act. She represents the very best of what it means to live, lead, and uplift others in spite of life’s challenges.

As you reflect on 106 years of impact, may this be a thrilling and profound moment — one that reminds you that your work echoes far beyond your walls, into the lives of real people, with real struggles, and real dreams.

Here’s to continued partnership, purpose, and progress. Happy Anniversary, JCSA!

We invite you to join our Lupus Support Group – Western Jamaica as we continue providing education, support, and empower...
25/03/2025

We invite you to join our Lupus Support Group – Western Jamaica as we continue providing education, support, and empowerment for individuals with lupus and their caregivers.

📅 Date: Wednesday, March 26, 2025
⏰ Time: 6:30 PM (Jamaica time)
📍 Where: Online via Zoom (Link will be provided upon request)

This session features Dr. Jonothan Ho, Consultant Dermatologist/Dermatopathologist,

who will discuss:
🔹 Lupus: What Does It Mean for My Skin?

Lupus can affect the skin in many ways, and this session will help you understand and manage these effects with expert advice.

📞 To receive the Zoom link, please reply to this email or call us at 876-840-7791.

Let’s continue to support each other on this journey. We look forward to seeing you there!

💜 What. A. Weekend! 💜From the laughter and bonding at our Youth Picnic to the moving performance of Basil Dawkins’ First...
24/03/2025

💜 What. A. Weekend! 💜

From the laughter and bonding at our Youth Picnic to the moving performance of Basil Dawkins’ First Lady Benefit Play, this past weekend was a beautiful mix of community, culture, and care. 🌞🎭

We want to say a massive THANK YOU to every single person who supported the process — from our planning teams to our volunteers, partners, sponsors, and each of you who showed up, spread the word, or simply held us in prayer.

Because of you:
🌸 Our youth lupus warriors had a safe space to connect and be themselves
🌸 Lupus awareness reached new hearts through the power of theatre
🌸 We were reminded that when we move together, we heal stronger

Here’s to continued collaboration, compassion, and community impact. We couldn’t do it without you. 🙏🏾💜

🎤 “Tell Me You Have Lupus Without Telling Me You Have Lupus” 💜At our recent Youth Picnic, our young lupus warriors took ...
24/03/2025

🎤 “Tell Me You Have Lupus Without Telling Me You Have Lupus” 💜

At our recent Youth Picnic, our young lupus warriors took on a challenge that was equal parts hilarious, heartfelt, and healing:

👉🏾 “Tell me you have lupus without telling me you have lupus.”

From witty one-liners about always carrying meds, to emotional nods to invisible pain and daily strength — every response was raw, real, and relatable.

It was a powerful moment of shared understanding, where warriors could express what it’s like to live with lupus in their own unique voice. Sometimes we don’t need to explain everything — we just need to be heard.

Big up to our brave warriors for showing up, speaking out, and reminding us that community and creativity go hand in hand on the journey. 💪🏾💜

💜 Happy International Women’s Day! 💜Today, as we celebrate the strength, resilience, and brilliance of women worldwide, ...
08/03/2025

💜 Happy International Women’s Day! 💜

Today, as we celebrate the strength, resilience, and brilliance of women worldwide, we also acknowledge the silent battles many women face; like lupus. Did you know that 90% of people living with lupus are women? This autoimmune disease disproportionately affects women, often striking in the prime of their lives, yet they continue to push forward with courage and grace.

💜 To the warriors who rise every day despite the pain—your strength is unmatched.
💜 To the caregivers, advocates, and researchers fighting for better treatment and awareness—you are changing lives.
💜 To every woman balancing dreams, responsibilities, and health challenges—you are seen, valued, and celebrated.

On this International Women’s Day, let’s not only honour the achievements of women but also raise awareness and stand in solidarity with those battling lupus and other chronic illnesses. Together, we can create a world where every woman has the support, resources, and recognition she deserves.

💜✨ Here’s to strong women—those who fight, those who uplift, and those who inspire. ✨💜

And to our sponsors who show up and show out, We appreciate you 🙌
07/03/2025

And to our sponsors who show up and show out, We appreciate you 🙌

💜 Love Yourself: Lupus Support Group Meeting – Tonight! 💜Self-care isn’t a luxury—it’s a necessity! Join us this evening...
20/02/2025

💜 Love Yourself: Lupus Support Group Meeting – Tonight! 💜

Self-care isn’t a luxury—it’s a necessity! Join us this evening for our Lupus Support Group Meeting as we explore the theme “Love Yourself”—a conversation about self-compassion, well-being, and prioritizing YOU.

📅 Date: Tonight, February 20, 2025
⏰ Log in at: 6:00 PM
📍 Where: Zoom (Link on flyer)

💜 What to Expect:
✔️ A safe, supportive space to connect with others in the lupus community
✔️ Self-care and mental wellness strategies tailored for lupus warriors
✔️ Encouragement, empowerment, and shared experiences

Whether you’re living with lupus or supporting a loved one, this session is for you! Let’s come together to uplift and inspire one another. See you soon!

🌿 Gratitude in Action: A Lifeline for Lupus Warriors 🌿Gratitude is more than words—it’s a powerful force that strengthen...
11/02/2025

🌿 Gratitude in Action: A Lifeline for Lupus Warriors 🌿

Gratitude is more than words—it’s a powerful force that strengthens the spirit and fuels resilience. For Lupus Warriors, it’s essential to staying well and thriving despite the challenges.

Today, the Lupus Foundation of Jamaica had the privilege of visiting Wysinco Group Limited, expressing our heartfelt thanks for over a decade of unwavering support. Even more inspiring, Wysinco reaffirmed their continued commitment to our mission—a true testament to the power of long-standing partnerships.

At the Foundation, gratitude isn’t just something we say; it’s how we live. It drives every support call, every shared victory, and every connection made with someone newly diagnosed. It keeps us grounded and pushes us forward.

Thank you, Wysinco, for walking this journey with us. Together, we continue to build a future of hope, strength, and community.

Address

Unit 29 Winchester Business Centre, 15 Hope Road, Kingston , Jamaica
Kingston
KINGSTON 10

Opening Hours

Monday 09:00 - 16:00
Tuesday 09:00 - 16:00
Wednesday 09:00 - 16:00
Thursday 09:00 - 16:00
Friday 09:00 - 16:00

Telephone

+18767548458

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